Rossi Vincenzo, Locatelli Sabrina, Varotto Serena, Donn Guenter, Pirona Raul, Henderson David A, Hartings Hans, Motto Mario
Consiglio per la Ricerca e Sperimentazione in Agricoltura, Istituto Sperimentale per la Cerealicoltura, Sezione di Bergamo, I-24126 Bergamo, Italy.
Plant Cell. 2007 Apr;19(4):1145-62. doi: 10.1105/tpc.106.042549. Epub 2007 Apr 27.
Enzymes catalyzing histone acetylation and deacetylation contribute to the modulation of chromatin structure, thus playing an important role in regulating gene and genome activity. We showed that downregulation and overexpression of the maize (Zea mays) Rpd3-type hda101 histone deacetylase gene induced morphological and developmental defects. Total levels of acetylated histones and histone acetylation of both repetitive and nonrepetitive sequences were affected in hda101 transgenic mutants. However, only transcript levels of genes but not repeats were altered. In particular, hda101 transgenic mutants showed differential expression of genes involved in vegetative-to-reproductive transition, such as liguleless2 and knotted-like genes and their repressor rough sheath2, which are required for meristem initiation and maintenance. Perturbation of hda101 expression also affected histone modifications other than acetylation, including histone H3 dimethylation at Lys-4 and Lys-9 and phosphorylation at Ser-10. Our results indicate that hda101 affects gene transcription and provide evidence of its involvement in setting the histone code, thus mediating developmental programs. Possible functional differences between maize hda101 and its Arabidopsis thaliana ortholog HDA19 are discussed.
催化组蛋白乙酰化和去乙酰化的酶有助于调节染色质结构,从而在调控基因和基因组活性中发挥重要作用。我们发现,玉米(Zea mays)Rpd3型组蛋白去乙酰化酶基因hda101的下调和过表达会诱导形态和发育缺陷。hda101转基因突变体中,重复序列和非重复序列的组蛋白乙酰化总水平以及组蛋白乙酰化均受到影响。然而,只有基因的转录水平发生了改变,重复序列的转录水平未变。特别是,hda101转基因突变体中参与营养生长向生殖生长转变的基因表现出差异表达,如叶舌缺失2和类结瘤基因及其抑制因子粗糙叶鞘2,这些基因是分生组织起始和维持所必需的。hda101表达的扰动还影响了除乙酰化以外的组蛋白修饰,包括赖氨酸-4和赖氨酸-9处的组蛋白H3二甲基化以及丝氨酸-10处的磷酸化。我们的结果表明,hda101影响基因转录,并为其参与设定组蛋白密码从而介导发育程序提供了证据。本文还讨论了玉米hda101与其拟南芥直系同源基因HDA19之间可能存在的功能差异。